Full data view for gene MYO7A


This database is one of the ”Retinal and hearing impairment genetic variant databases”.
Information The variants shown are described using the NM_000260.3 transcript reference sequence.

12 entries on 1 page. Showing entries 1 - 12.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

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Owner     
+/+ 3 c.73G>A r.(?) p.(Gly25Arg) Motor domain (1-729) Paternal (confirmed) - pathogenic g.76853809G>A g.77142763G>A - - MYO7A_000134 Heterozygous PubMed: Le Quesne Stabej 2012; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/878 controls none - - DNA SEQ - - USH1 - PubMed: Le Quesne Stabej 2012 Proband - - United Kingdom (Great Britain) - - - - - 1 Maria Bitner-Glindzicz
+/+ 3 c.73G>A r.(?) p.(Gly25Arg) Motor domain (1-729) Parent #2 - pathogenic g.76853809G>A g.77142763G>A - - MYO7A_000134 Heterozygous PubMed: Levy 1997; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/100 controls none - - DNA SEQ - - USH1B ? PubMed: Levy 1997 Proband - - United Kingdom (Great Britain) - - - - - 1 Anne-Françoise Roux
+/+ 3 c.73G>A r.(?) p.(Gly25Arg) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76853809G>A g.77142763G>A - - MYO7A_000134 Heterozygous; mutation PubMed: Gao 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/438 controls none - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Gao 2014 Proband M - China - - - - - 1 Anne-Françoise Roux
+/+ 3 c.73G>A r.(?) p.(Gly25Arg) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76853809G>A g.77142763G>A - - MYO7A_000134 Heterozygous; mutation PubMed: Gao 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/438 controls none - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Gao 2014 Relative F - China - - - - - 1 Anne-Françoise Roux
+/+ 3 c.73G>A r.(?) p.(Gly25Arg) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76853809G>A g.77142763G>A - - MYO7A_000134 Heterozygous; mutation PubMed: Gao 2014; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - 0/438 controls none - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Gao 2014 Relative M - China - - - - - 1 Anne-Françoise Roux
+/+ 3 c.73G>A r.(?) p.(Gly25Arg) Motor domain (1-729) Maternal (confirmed) - pathogenic g.76853809G>A g.77142763G>A - - MYO7A_000134 Heterozygous PubMed: Lenarduzzi 2015; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - none - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Lenarduzzi 2015 Proband - - Italy - - - - - 1 Anne-Françoise Roux
+/+ 3 c.73G>A r.(?) p.(Gly25Arg ) Motor domain (1-729) Parent #2 - pathogenic g.76853809G>A g.77142763G>A - - MYO7A_000134 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - France - - - - - 1 Crystel Bonnet
+/+ 3 c.73G>A r.(?) p.(Gly25Arg ) Motor domain (1-729) Parent #1 - pathogenic g.76853809G>A g.77142763G>A - - MYO7A_000134 Heterozygous; mutation PubMed: Bonnet 2016; USMA-USMA missense analysis USMA-missense variant in MSV3d - - Germline - - - - - DNA SEQ, SEQ-NG-S - - USH1B ? PubMed: Bonnet 2016 Proband M - Italy - - - - - 1 Crystel Bonnet
+/. 3 c.73G>A r.(?) p.(Gly25Arg) - Both (homozygous) ACMG pathogenic (recessive) g.76853809G>A - - - MYO7A_000134 - PubMed: Bahena 2021 - - Germline yes - - - - DNA SEQ-NG-IT - Exome sequencing USH1B Pat2 PubMed: Bahena 2021 - M yes Iran - - - - - 2 Barbara Vona
+/. - c.73G>A r.(?) p.(Gly25Arg) - Unknown - pathogenic g.76853809G>A - - - MYO7A_000134 - - - rs782252317 CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
+/. - c.73G>A r.(?) p.(Gly25Arg) - Unknown ACMG pathogenic g.76853809G>A - - - MYO7A_000134 - PubMed: Mansard et al, 2021 - rs782252317 Germline - - - - - DNA SEQ-NG, SEQ - - USH1 - PubMed: Mansard et al, 2021 - F - - - - - - - 1 Anne-Françoise Roux
+?/. 3 c.73G>A r.(?) p.(Gly25Arg) - Paternal (confirmed) - likely pathogenic (recessive) g.76853809G>A - c.73G>A - MYO7A_000134 - PubMed: Khateb 2020 - - Germline - - - - - DNA ? - - retinal disease CIC07289 PubMed: Khateb 2020 one affected daughter M yes - Father Moroccan and mother French - - - - 1 LOVD
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